Tan Hui-Hui, Chow Wan-Cheng, Lim Kiat-Hon, Wan Wei-Keat, Chung Alexander Y F, Cheow Peng-Chung, Tan Chee-Kiat
Liver Transplant Service, Department of Gastroenterology and Hepatology, Singapore General Hospital, Singapore 169608.
J Transplant. 2011;2011:176370. doi: 10.1155/2011/176370. Epub 2011 May 10.
Citrullinaemia is a urea cycle defect that results from a deficiency of the enzyme arginosuccinate synthetase. Type 1 disease is diagnosed in childhood, whereas Type 2 disease is adult onset. We report the outcome of a patient with citrullinemia Type 2 who received a liver transplant at our center and the implications of this diagnosis in liver transplantation.
瓜氨酸血症是一种尿素循环缺陷病,由精氨琥珀酸合成酶缺乏引起。1型疾病在儿童期被诊断,而2型疾病为成人发病。我们报告了一名在本中心接受肝移植的2型瓜氨酸血症患者的治疗结果以及该诊断在肝移植中的意义。